Belgif Linked Data Fragments server

Matches in Data.gov.be for { <http://data.gov.be/.well-known/genid/cfcba76b740b4245a85ec359572ede9e2-b2348> ?p ?o ?g. }

• cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Ulnar-mammary syndrome" @default.
• cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Unverricht-Lundborg disease" @default.
• cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Usher syndrome" @default.
• cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Van der Woude syndrome" @default.
• cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Vascular Ehlers-Danlos syndrome" @default.
• cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Vitiligo-associated autoimmune disease" @default.
• cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Von Hippel-Lindau disease" @default.
• cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome" @default.
• cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "WAGR syndrome" @default.
• cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Waardenburg syndrome" @default.
• cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Waardenburg-Shah syndrome" @default.
• cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Wiedemann-Steiner syndrome" @default.
• cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Williams syndrome" @default.
• cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Wilson disease" @default.
• cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Wolf-Hirschhorn syndrome" @default.
• cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Wolfram syndrome" @default.
• cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Wolfram-like syndrome" @default.
• cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "X-linked Alport syndrome-diffuse leiomyomatosis" @default.
• cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "X-linked Charcot-Marie-Tooth disease type 1" @default.
• cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "X-linked Charcot-Marie-Tooth disease type 2" @default.
• cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "X-linked Charcot-Marie-Tooth disease" @default.
• cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "X-linked ichthyosis syndrome" @default.
• cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "X-linked intellectual disability-hypotonia- movement disorder syndrome" @default.
• cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "X-linked intellectual disability-hypotonia-facial dysmorphism-aggressive behavior syndrome" @default.
• cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Xq25 microduplication syndrome" @default.
• cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Zellweger syndrome" @default.
• cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "autosomal dominant Charcot-Marie-Tooth disease type 2 due to KIF5A mutation" @default.
• cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "autosomal dominant Charcot-Marie-Tooth disease type 2J" @default.
• cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "autosomal dominant Charcot-Marie-Tooth disease type 2W" @default.
• cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "autosomal dominant intellectual disability- craniofacial anomalies-cardiac defects syndrome" @default.
• cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "autosomal dominant intermediate Charcot- Marie-Tooth disease type E" @default.
• cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis" @default.
• cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "autosomal dominant polycystic kidney disease" @default.
• cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "autosomal dominant tubulointerstitial kidney disease" @default.
• cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "autosomal ichthyosis syndrome" @default.
• cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "autosomal recessive multiple pterygium syndrome" @default.
• cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "autosomal recessive polycystic kidney disease" @default.
• cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "congenital and infantile nephrotic syndrome" @default.
• cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome" @default.
• cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "congenital myasthenic syndrome" @default.
• cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "congenital nephrotic syndrome- Finnish type" @default.
• cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "distal 16p11.2 microdeletion syndrome" @default.
• cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "distal 17p13.3 microdeletion syndrome" @default.
• cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "distal 22q11.2 microdeletion syndrome" @default.
• cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "distal 22q11.2 microduplication syndrome" @default.
• cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "distal Xq28 microduplication syndrome" @default.
• cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "hereditary arterial and articular multiple calcification syndrome" @default.
• cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "hereditary breast and ovarian cancer syndrome" @default.
• cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "neuromuscular disease" @default.
• cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "sickle cell-hemoglobin SS disease" @default.
• cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "syndrome de Turner" @default.
• cfcba76b740b4245a85ec359572ede9e2-b2348 landingPage a36012ab-8ab5-4fcf-b86c-c5c191ad14b0 @default.
• cfcba76b740b4245a85ec359572ede9e2-b2348 theme HEAL @default.

• first
• previous